Trifluoroacetic acid → 2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetal

HRID 898638Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 898638
[CH:1](=O)[CH2:2][CH2:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[CH3:12][O:13][CH:14]([O:17][CH3:18])[CH2:15][NH2:16].[BH3-]C#N.[Na+].C(O)(C(F)(F)F)=O>CO>[CH3:12][O:13][CH:14]([O:17][CH3:18])[CH2:15][NH:16][CH2:1][CH2:2][CH2:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Komponenten

6

Versuchsvorschrift

trans-4-Decenal (7.2 g, 46.6 mmol) was mixed with 40 mL (0.37 moL) of aminoacetaldehyde dimethylacetal in 400 mL of methanol and stirred at room temperature for 30 minutes. NaCNBH3 (2.9 g, 46.6 mmol) was added, the reaction was cooled in an ice bath, and 27 mL (0.35 moL) of TFA was added dropwise over 5 minutes. The ice bath was then removed and the reaction was stirred for 70 minutes at room temperature, concentrated to a third of its volume, and partitioned between ethyl acetate (250 mL) and 1N NaOH (200 mL). The organic layer was washed with water (3×75 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield 11.1 g (45.6 mmol) of 2-(trans-dec-4-en-1-ylamino)acetaldehyde dimethyl acetal as a yellow oil that was used directly in the next step.

Aufarbeitung

  1. temperaturethe reaction was cooled in an ice bath
  2. customThe ice bath was then removed
  3. stirringthe reaction was stirred for 70 minutes at room temperature
  4. concentrationconcentrated to a third of its volume
  5. custompartitioned between ethyl acetate (250 mL) and 1N NaOH (200 mL)
  6. washThe organic layer was washed with water (3×75 mL)
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3534b6b35527498983a1a7d9e8557249
Quelldatensatz
uspto-grants-2008_04
Patentnummer
US07351791B2

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